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Sodium 2-(1-naphthyl)hex-4-enoate

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Identification
Molecular formula
C16H15NaO2
CAS number
867-16-1
IUPAC name
sodium;2-(1-naphthyl)hex-4-enoate
State
State

At room temperature, sodium 2-(1-naphthyl)hex-4-enoate is typically encountered as a solid. It may present itself in a crystalline form or as a fine powder.

Melting point (Celsius)
120.60
Melting point (Kelvin)
393.75
Boiling point (Celsius)
318.70
Boiling point (Kelvin)
591.85
General information
Molecular weight
260.29g/mol
Molar mass
260.3080g/mol
Density
1.1625g/cm3
Appearence

The compound typically appears as a white to off-white solid. Its appearance may be consistent with that of a fine powder or crystalline substance.

Comment on solubility

Solubility of Sodium 2-(1-naphthyl)hex-4-enoate

Sodium 2-(1-naphthyl)hex-4-enoate is a unique compound known for its intriguing solubility characteristics. Understanding its solubility helps in comprehending its behavior in various environments. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is likely to be soluble in organic solvents due to the presence of the naphthyl group, which is hydrophobic in nature.
  • Aqueous Solubility: The sodium salt form generally enhances solubility in water, given that sodium ions often increase the polarity of organic molecules.
  • Temperature Dependence: As with many chemical compounds, solubility may vary with temperature; increased temperatures can often enhance solubility in solvents.
  • pH Influence: The solubility of anionic compounds like sodium 2-(1-naphthyl)hex-4-enoate may vary with the pH of the solution, affecting the degree of ionization.
  • Complexation: The presence of potential coordinating moieties in the structure may lead to complexation with certain metal ions, which could either enhance or diminish solubility.

In summary, the solubility of sodium 2-(1-naphthyl)hex-4-enoate is characterized by a combination of hydrophobic and hydrophilic interactions. Thus, it is crucial to consider the solvent system and environmental conditions when assessing its solubility properties.

Interesting facts

Interesting Facts about Sodium 2-(1-Naphthyl)hex-4-enoate

Sodium 2-(1-naphthyl)hex-4-enoate, a fascinating chemical compound, possesses unique properties and structures that make it a subject of interest in scientific research.

Key Characteristics

  • Dual Functional Groups: This compound contains both a sodium salt and an alkene functionality, which enhances its reactivity and potential applications in organic synthesis.
  • Conjugated System: The presence of the naphthyl group introduces a conjugated system, contributing to its electronic properties and making it a suitable candidate for studies in photochemistry.
  • Biological Relevance: Compounds that include naphthyl units are often associated with biological activities, including antimicrobial and antitumor effects. This raises intriguing questions about the biological significance of sodium 2-(1-naphthyl)hex-4-enoate.

Applications and Uses

The unique structure of sodium 2-(1-naphthyl)hex-4-enoate opens up various avenues for its application:

  • Organic Synthesis: It can act as a building block in the synthesis of more complex organic molecules.
  • Dyes and Pigments: Naphthalene derivatives, like this compound, are often used in the production of dyes due to their vibrant colors and stability.
  • Research and Development: Scientists explore such compounds for their potential use in creating new materials, particularly in areas like semiconductors and solar cells.

Quote from the Scientific Community

As noted by chemists, “The study of naphthyl compounds like sodium 2-(1-naphthyl)hex-4-enoate enriches our understanding of organic chemistry and expands the toolkit available for chemical invention.”

In summary, sodium 2-(1-naphthyl)hex-4-enoate stands out for its intriguing structure and diverse potential applications, making it a valuable compound in both academic and industrial chemistry. Its dual properties not only deepen our understanding of chemical reactivity but also pave the way for innovative developments in chemical research.